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Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars-Sinai Medical Center

Los Angeles, California

Cedars Sinai

Los Angeles, California

TRIO-US, Inc.

Los Angeles, California

University of Illinois Cancer Center

Chicago, Illinois

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Slone Partners

North Charleston, South Carolina

Asher Biotherapeutics

South San Francisco, California

Asher Biotherapeutics

South San Francisco, California

Northeast Georgia Health System

Gainesville, Georgia

Stanford, School of Medicine

Palo Alto, California

Stanford, School of Medicine

Palo Alto, California

WellNow Clinical Research

Columbus, Ohio

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URMC Clinical & Translational Science Institute Office of Clinical Research

Rochester, New York

University of Illinois Cancer Center

Chicago, Illinois

Lakeland Regional Health

Lakeland, Florida

North Georgia Clinical Research

Woodstock, Georgia

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Arthrex

Naples, Florida

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IRB Research Monitor
IRB Research Monitor IRB Research MonitorRequired Qualifications (as evidenced by an attached resume):Bachelor's degree (foreign equivalent or higher). In lieu of a Bachelor's degree, a combination of relevant higher education and experience totaling four (4) years may be considered. Three (3) years of full time IRB/regulatory experience. Experience with Microsoft Office and/or Google applications.Preferred Qualifications:Experience in a human subjects protection program. Experience with AAHRPP standards and accreditation requirements. Experience with the Health


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